Yingying Wu1, Fuwei Liu2, Xiang Zhang2, Lei Shu3. 1. Department of Dentistry, Chinese PLA General Hospital, Beijing 100853, China. 2. Department of Prosthodontics, School of Stomatology, Fourth Military Medical University, Xi'an 710032, China. 3. Department of Dentistry, 101 Hospital of Chinese People's Liberation Army, Wuxi 214044, China. Electronic address: leishumd@gmail.com.
Abstract
OBJECTIVE: Periodontal disease (PD) has recently been recognized as the 'sixth' major complication of diabetes but the mechanisms involved in diabetic PD remain unclear. This study was to elucidate the potential bone-sparing effect of insulin in diabetic PD conditions. DESIGN: The human periodontal ligament (hPDL) cells were obtained from the healthy hPDL tissue and were treated with high concentrations (25 or 45mM) of glucose with or without different concentrations (10(-6), 10(-7) or 10(-8)mM) of insulin. RESULTS: High concentrations of glucose increased the production of pro-inflammatory cytokines interleukin-1 beta (IL-1β), tumour necrosis factor alpha (TNF-α), Interleukin-6 (IL-6) at both mRNA and protein levels, and receptor activator of NF-кB ligand (RANKL) at mRNA levels in hPDL cells. Insulin treatment alleviated the stimulatory effects of high glucose on pro-inflammatory cytokines and RANKL expression by hPDL cells. Moreover, insulin up-regulated OPG expression and therefore attenuated the reduction of OPG vs. RANKL ratio. CONCLUSION: Insulin plays significant roles in modulating the periodontal tissue responses to hyperglycemia, and thus exerts its bone-sparing effects on periodontal tissues via altering the inflammatory cytokines expression in hPDL cells.
OBJECTIVE: Periodontal disease (PD) has recently been recognized as the 'sixth' major complication of diabetes but the mechanisms involved in diabetic PD remain unclear. This study was to elucidate the potential bone-sparing effect of insulin in diabetic PD conditions. DESIGN: The human periodontal ligament (hPDL) cells were obtained from the healthy hPDL tissue and were treated with high concentrations (25 or 45mM) of glucose with or without different concentrations (10(-6), 10(-7) or 10(-8)mM) of insulin. RESULTS: High concentrations of glucose increased the production of pro-inflammatory cytokines interleukin-1 beta (IL-1β), tumour necrosis factor alpha (TNF-α), Interleukin-6 (IL-6) at both mRNA and protein levels, and receptor activator of NF-кB ligand (RANKL) at mRNA levels in hPDL cells. Insulin treatment alleviated the stimulatory effects of high glucose on pro-inflammatory cytokines and RANKL expression by hPDL cells. Moreover, insulin up-regulated OPG expression and therefore attenuated the reduction of OPG vs. RANKL ratio. CONCLUSION:Insulin plays significant roles in modulating the periodontal tissue responses to hyperglycemia, and thus exerts its bone-sparing effects on periodontal tissues via altering the inflammatory cytokines expression in hPDL cells.
Authors: Hasaan G Mohamed; Shaza B Idris; Mutaz F Ahmed; Anne N Åstrøm; Kamal Mustafa; Salah O Ibrahim; Manal Mustafa Journal: BMC Oral Health Date: 2015-07-27 Impact factor: 2.757